Registry of long-term antithrombotic therapy for atrial fibrillation

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to evaluate the rates of ischemic and hemorrhagic complications associated with long-term antithrombotic therapy in patients diagnosed with atrial fibrillation. Conducted at a single center in Russia, the study will involve patients who meet specific criteria for antithrombotic treatment. By documenting outcomes over time, the study seeks to provide insights into the safety and efficacy of anticoagulants in this patient population.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Documented atrial fibrillation with CHA2DS2VASC \> 1

Exclusion Criteria:

* Subjects who are unwilling or unable to provide informed consent. ACS within 12 months before inclusion Severe CHF (NYHA IV) Stroke within 6 months before inclusion Severe liver or muscle disease Severe kidney disease / renal failure with creatinine \> 3 mg/dl Conceivable impossibility to come in touch with the patient or his family at 1-year after the intervention

Where it's running

• National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
  Moscow, Russia Recruiting

Study contacts

• Principal investigator: Elizaveta Panchenko, PhD — National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
• Study coordinator: Ekaterina Kropacheva, PhD
• Email: katekrab@list.ru
• Phone: +79166760695

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.